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US9050286B2 - Use of peptidic vasopression receptor agonists - Google Patents

Use of peptidic vasopression receptor agonists Download PDF

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Publication number
US9050286B2
US9050286B2 US12/673,375 US67337508A US9050286B2 US 9050286 B2 US9050286 B2 US 9050286B2 US 67337508 A US67337508 A US 67337508A US 9050286 B2 US9050286 B2 US 9050286B2
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induced
compound
syndrome
alkyl
shock
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US20110237494A1 (en
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Regent Laporte
Pierre J-M Riviere
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Ferring BV
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Ferring BV
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/12—Cyclic peptides, e.g. bacitracins; Polymyxins; Gramicidins S, C; Tyrocidins A, B or C
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/08—Plasma substitutes; Perfusion solutions; Dialytics or haemodialytics; Drugs for electrolytic or acid-base disorders, e.g. hypovolemic shock
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04—Linear peptides containing only normal peptide links
    • C07K7/16—Oxytocins; Vasopressins; Related peptides

Definitions

  • the present invention relates to the use of novel compounds for the manufacture of a medicament for treatment of inter alia conditions associated with critical care as well as to a method for treatment of said conditions, wherein said compounds are administered.
  • Peptidic vasopressin V1a receptor agonists such as terlipressin
  • terlipressin have recently (see e.g. O'Brian et al., Lancet 359 (9313):1209-10, Jun. 4, 2002) received increased attention for clinical use in treatment of critical care diseases and conditions, including shock of hypovolemic (e.g. hemorrhagic) or vasodilatory (e.g. septic) origin, bleeding esophageal varices (BEV), hepatorenal syndrome (HRS), cardiopulmonary resuscitation and anesthesia-induced hypotension.
  • shock of hypovolemic e.g. hemorrhagic
  • vasodilatory e.g. septic
  • BEV bleeding esophageal varices
  • HRS hepatorenal syndrome
  • cardiopulmonary resuscitation e.g. pneumopressin V1a receptor agonists
  • terlipressin in many critical care situations is its long duration of action, which makes it difficult to titrate its effect as the disease state changes.
  • Terlipressin metabolites have agonist activity at the human V1a (hV1a) receptor.
  • F180 (cf. example 3 in U.S. Pat. No. 5,459,236) has an inconveniently long duration of action to be considered for the treatment of most critical care conditions.
  • Non-specific receptor agonist activity is the main disadvantage of other existing compounds, e.g. [Phe2,Orn8]OT (cf. example if in U.S. Pat. No. 3,352,843) and arginine-vasopressin (AVP).
  • Activity at related receptors such as V1b, V2 and oxytocin (OT) receptors may potentially generate undesirable side effects and safety concerns.
  • V2 receptor activation may induce antidiuresis (cf. desmopressin), release of coagulation/thrombolysis factors, and induce vasodilation/hypotension with reflex tachycardia. The latter side effect may also be induced by OT receptor agonist activity.
  • the present invention relates to the use of compounds represented by the general formula (I):
  • R 1 is selected from H and part of an alicyclic structure that comprises from 3 to 8 carbon atoms
  • R 2 is selected from (CH 2 ) m —X and part of said alicyclic structure
  • m is selected from 0, 1, 2 and 3
  • n is selected from 0, 1, 2, 3 and 4
  • p is selected from 2, 3 and 4
  • X is selected from C 3-8 -cycloalkyl, C 5-8 -cycloalkenyl and C 5-8 -cycloalkynyl
  • when m is 1, X is selected from C 3-8 -cycloalkyl, C 5-8 -cycloalkenyl, C 5-8 -cycloalkynyl, isopropyl and tert-butyl; said alicyclic structure
  • ARDS acute respiratory distress syndrome
  • ALI acute lung injury
  • Still further uses of the above compounds are for the manufacture of a medicament for treatment of inadequate tissue oxygenation, e.g. stemming from nitrogen intoxication (hypoxic lactic acidosis) or carbon monoxide intoxication, shock induced by metformin intoxication, mitochondrial disease or cyanide poisoning, vascular leak syndrome (VLS) induced by interleukin-2 (IL-2) or other cytokines, denileukin diftitox or other immunotoxins, or ovarian hyperstimulation syndrome (OHSS), hypertension induced by end-stage renal disease (ESRD), severe burns, thermal injury, irritable bowel disease (IBD), including Crohn's disease and ulcerative colitis, reperfusion injury (e.g.
  • inadequate tissue oxygenation e.g. stemming from nitrogen intoxication (hypoxic lactic acidosis) or carbon monoxide intoxication, shock induced by metformin intoxication, mitochondrial disease or cyanide poisoning, vascular leak syndrome (VLS)
  • vasodepressor syncope e.g. vasovagal syncope, postural hypotension with syncope or neurocardiogenic syncope, toxic shock syndrome, idiopathic systemic capillary leak syndrome (Clarkson's disease).
  • C 1-6 denotes having from one to six carbon atoms, including any number therebetween, and this nomenclature is used analogously herein.
  • Examples of pharmaceutically acceptable salts comprise acid addition salts, e.g. a salt formed by reaction with hydrohalogen acids, such as hydrochloric acid, and mineral acids, such as sulphuric acid, phosphoric acid and nitric acid, as well as aliphatic, alicyclic, aromatic or heterocyclic sulphonic or carboxylic acids, such as formic acid, acetic acid, propionic acid, succinic acid, glycolic acid, lactic acid, malic acid, tartaric acid, citric acid, ascorbic acid, maleic acid, hydroxymaleic acid, pyruvic acid, p-hydroxybenzoic acid, embonic acid, methanesulphonic acid, ethanesulphonic acid, hydroxyethanesulphonic acid, halobenzenesulphonic acid, toluenesulphonic acid and naphtalenesulphonic acid.
  • hydrohalogen acids such as hydrochloric acid
  • mineral acids such as sulphuric acid, phosphoric acid and
  • R 7 and R 8 are H. It is especially preferred that R 3 and R 4 are H.
  • n is 1 or 2.
  • Alkyl is typically selected from methyl, ethyl, n-propyl, i-propyl, t-butyl and i-amyl.
  • X is preferably selected from cyclopentyl and cyclohexyl.
  • Said alicyclic structure is preferably a cyclobutyl structure.
  • said compound having the formula (I) is selected from a group consisting of:
  • the pharmaceutical composition used when practising the present invention may be adapted for oral, intravenous, topical, intraperitoneal, nasal, buccal, sublingual or subcutaneous administration or for administration via the respiratory tract e.g. in the form of an aerosol or an air-suspended fine powder.
  • the composition may thus for instance be in the form of tablets, capsules, powders, microparticles, granules, syrups, suspensions, solutions, transdermal patches or suppositories.
  • the pharmaceutical composition used may optionally comprise e.g. at least one further additive selected from a disintegrating agent, binder, lubricant, flavoring agent, preservative, colorant and any mixture thereof.
  • a further additive selected from a disintegrating agent, binder, lubricant, flavoring agent, preservative, colorant and any mixture thereof. Examples of such and other additives are found in “ Handbook of Pharmaceutical Excipients ”; Ed. A. H. Kibbe, 3 rd Ed., American Pharmaceutical Association, USA and Pharmaceutical Press UK, 2000.
  • the pharmaceutical composition used is most preferably adapted for parenteral administration. It may comprise a sterile aqueous preparation of the compounds of the invention preferably isotonic with the blood of the recipient.
  • This aqueous preparation may be formulated according to known methods using suitable dispersing or wetting agents and suspending agents.
  • the injectable aqueous formulation Remestyp® (terlipressin) is exemplary of a suitable pharmaceutical formulation type.
  • the preparation may also be a sterile injectable solution or suspension in a diluent or solvent, for example as a solution in 1,3-butane diol. Water, Ringer's solution, and isotonic sodium chloride solution are exemplary acceptable diluents.
  • Sterile, fixed oils may be employed as a solvent or suspending medium. Bland fixed oils, including synthetic mono or di-glycerides, and fatty acids, such as oleic acid, may also be used.
  • the invention in another embodiment relates to a method for treatment of hypertensive gastropathy bleeding, sepsis, severe sepsis, septic shock, prolonged and severe hypotension, intradialytic hypotension, cardiac arrest, trauma related blood loss, vasodilatory shock induced by cardio-pulmonary bypass, milrinone-induced vasodilatory shock in congestive heart failure, hepatorenal syndrome type I, anaphylactic shock, or cardiovascular instability induced by brain death, wherein said method comprises administering to an animal, including human, patient of a therapeutically effective amount of a compound as outlined above.
  • the invention relates to a method for treatment of hypotension in severe sepsis, acute respiratory distress syndrome or acute lung injury, wherein said method comprises administering to an animal, including human, patient of a therapeutically effective amount of a compound as outlined above.
  • the invention in another embodiment relates to a method for treatment of inadequate tissue oxygenation, shock induced by metformin intoxication, mitochondrial disease or cyanide poisoning, vascular leak syndrome induced by interleukin-2 or other cytokines, denileukin diftitox or other immunotoxins, or ovarian hyperstimulation syndrome, hypertension induced by end-stage renal disease, severe burns, thermal injury, irritable bowel disease, ulcerative colitis, reperfusion injury, infant respiratory distress syndrome, severe acute respiratory syndrome, ascites, vasodepressor syncope, including vasovagal syncope, postural hypotension with syncope or neurocardiogenic syncope, toxic shock syndrome, idiopathic systemic capillary leak syndrome (Clarkson's disease), wherein said method comprises administering to an animal, including human, patient of a therapeutically effective amount of a compound as outlined above.
  • the typical dosage of the compounds used according to the present invention varies within a wide range and will depend on various factors such as the individual needs of each patient and the route of administration.
  • the dosage administered by infusion is generally within the range of 0.01-200 mg/kg body weight per hour. A physician of ordinary skill in the art will be able to optimise the dosage to the situation at hand.
  • Amino acid derivatives and resins were purchased from commercial providers (Novabiochem, Bachem, Peptide International and PepTech Corporation). Other chemicals and solvents were provided from Sigma-Aldrich, Fisher Scientific and VWR.
  • Purity of the synthesized peptide may be determined by analytical reversed phase HPLC. Structural integrity of the peptides may be confirmed using amino acid analysis and electrospray mass spectrometry.
  • the peptides synthesised by Fmoc methodology were cleaved with a TFA/TIS/H 2 O 96/2/2 (v/v/v) solution, and cleavage in Boc methodology was accomplished with 90% HF/10% anisole (v/v) solution.
  • Disulfide bridge (ring) formation was achieved by oxidation of linear peptides dissolved in 10% TFA (aq) with iodine.
  • Peptides were purified by preparative HPLC in triethylammonium phosphate buffers (aq). The compounds were finally converted to acetate salts using conventional HPLC methodology. The fractions with a purity exceeding 97% were pooled and lyophilised.
  • the peptides were assembled with Fmoc methodology.
  • the diamino acid residue in position no. 8 was introduced with an acid labile (i.e. removable with a solution containing 1-2% TFA) protecting group, such as methoxytrityl (Mmt; see Barlos, K. et al. in Peptides 1992, Schneider, C. H., Eberle, A. N., Eds., ESCOM Science Publishers B.V., 1993, pp 283-284).
  • Resin bound peptide was treated with a DCM/TIS/TFA 93/5/2 (v/v/v) solution for the Mmt group removal.
  • Reductive alkylation with acetone/NaBH(OAc) 3 provided the N-isopropyl peptide.
  • the peptides were assembled with Boc methodology.
  • the residue in position no. 4 was introduced in the sequence as Boc-Asp(OFm)-OH.
  • the side chain protection was removed with 30% piperidine in DMF.
  • the resulting free carboxylic group was converted to the desired amide by coupling with an appropriate amine mediated by PyBOP or BOP/DIEA.
  • the N-terminal Boc group was then removed, followed by HF cleavage, cyclisation and purification by HPLC.
  • Table 1 lists the compounds prepared by the above procedure together with the determined (vide infra) EC 50 (median effective concentration) expressed in nanomol/L.
  • R 3 , R 4 , R 5 , R 6 , R 7 and R 6 are H for all compounds except compound 4, where R 6 is isopropyl instead of H.
  • m is 1, except where R 1 and R 2 are part of an alicyclic structure (formed together with the a carbon of the amino acid in position no. 2) exemplified here as 1,1-cyclobutyl.
  • amino acid derivatives used were Boc-Cys(Trt)-OH, Fmoc-Cha-OH, Fmoc-Ile-OH, Fmoc-Gln(Trt)-OH, Fmoc-Asn(Trt)-OH, Fmoc-Cys(Trt)-OH, Fmoc-Pro-OH, Fmoc-Orn(Mmt)-OH and Fmoc-Gly-OH.
  • Analytical HPLC was performed on a Waters 600 Liquid Chromatograph using a Vydac C18, 5 ⁇ 4.6 ⁇ 250 mm, column at a flow rate of 2 ml/min.
  • Preparative HPLC was performed on a Waters 2000 Liquid Chromatograph using a Prepak 47 ⁇ 300 mm cartridge at a flow rate of 100 ml/min.
  • Final compound analysis was performed on a 1100 Agilent Liquid Chromatograph using a Vydac C18, 5 ⁇ 2.1 ⁇ 250 mm, column at a flow rate of 0.3 ml/min. Mass spectra were recorded on a Finnigan MAT spectrometer.
  • the fully protected peptide resin was synthesised on an Applied Biosystems 9050 Peptide Synthesiser starting from 0.4 g (0.1 mmol) of Tentagel-S-RAM resin (Peptides International). DIC/HOBt mediated single couplings with a 4-fold excess of amino acid derivatives were performed. The Fmoc group was removed with 20% piperidine in DMF. Upon completion of the automated synthesis, the resin was transferred into a manual synthesis vessel and was treated with DCM/TIS/TFA 93/5/2 (v/v/v) solution (30 ml) for 2 ⁇ 1.5 hours for removal of the Mmt group.
  • the resin was thoroughly washed with DCM and was subsequently suspended in 15 ml of 1,2-dichloroethane/TMOF 1:1 (v/v). 0.2 ml of acetone was then added followed by 0.6 g of NaBH(OAc) 3 . The suspension was shaken overnight and the resin was washed with methanol, DMF and DCM and dried in vacuo. The resin was then treated with 30 ml of the TFA/TIS/H 2 O 96/2/2 (v/v/v) solution for 1.5 hours and filtered off. The filtrate was evaporated and the crude linear peptide was precipitated with diethyl ether.
  • the precipitate was immediately dissolved in 500 ml of 10% TFA (aq), and the peptide was oxidised by adding 0.1 M I 2 in methanol to the magnetically stirred solution until yellow color persisted. Excess of iodine was reduced with ascorbic acid. The reaction mixture was then cooled with crushed ice and pH was adjusted to about 5 by adding concentrated ammonia (aq). The mixture was loaded onto an HPLC column and purified using a triethylammonium phosphate buffer with pH 5.2. The compound was eluted with a gradient of acetonitrile. The fractions with a purity exceeding 97% were pooled, and the resulting solution was diluted with 2 volumes of water.
  • amino acid derivatives used were Boc-Cys(Mob)-OH, Boc-AcBuc-OH, Boc-Ile-OH, Boc-Gln-OH, Boc-Asn-OH, Boc-Pro-OH, Boc-Dbu(Z)—OH DCHA salt and Boc-Gly-OH, all purchased from Novabiochem and Bachem. HPLC and MS operations were performed as in the synthesis of 202256.
  • the fully protected peptide resin was manually synthesised starting from 0.6 g (0.4 mmol) of 4-methylbenzhydrylamine resin (Novabiochem). DCC, PyBOP or DIC/HOBt mediated single couplings with 2.5-fold excess of amino acid derivatives were employed.
  • the Boc group was removed with 50% TFA in DCM containing 1% of m-cresol.
  • the finished resin was washed with methanol, DMF and DCM and dried in vacuo.
  • the peptide was cleaved from the resin by using 30 ml of anhydrous HF containing 3 ml of anisole at 0° C. for 90 minutes. The HF was evaporated off, and the crude linear peptide was washed with diethyl ether.
  • the peptide was immediately dissolved in 200 ml of 25% acetonitrile/10% TFA (aq) and oxidised as described supra. The resulting mixture was loaded directly onto an HPLC column and purified using triethylammonium phosphate buffer at pH 2.3. Unless otherwise provided the subsequent steps were identical to the procedure for 202256. 80.6 mg (22% yield) of white amorphous powder was obtained.
  • Agonist activity of compounds on the hV1a receptor was determined in a transcriptional reporter assay by transiently transfecting a hV1a receptor expression DNA into HEK-293 cells in concert with a reporter DNA containing intracellular calcium responsive promoter elements regulating expression of firefly luciferase. See Boss, V., Talpade, D. J., Murphy, T. J. J. Biol. Chem. 1996, May 3; 271(18), 10429-10432 for further guidance on this assay. Cells were exposed to serial dilutions of compounds diluted 10-fold per dose for 5 hours, followed by lysis of cells, determination of luciferace activity, and determination of compound efficacies and EC 50 values through non-linear regression. Arginine-vasopressin (AVP) was used as an internal control in each experiment, and compounds were tested in at least three independent experiments.
  • AVP Arginine-vasopressin

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US12/673,375 2007-08-14 2008-08-08 Use of peptidic vasopression receptor agonists Expired - Fee Related US9050286B2 (en)

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PCT/IB2008/003444 WO2009037586A2 (fr) 2007-08-14 2008-08-08 Utilisation d'agonistes peptidiques du récepteur de la vasopressine
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JP5185830B2 (ja) * 2006-02-10 2013-04-17 フェリング ベスローテン フェンノートシャップ 新規化合物
PL3209317T3 (pl) 2014-10-24 2022-05-23 Mallinckrodt Pharmaceuticals Ireland Limited Terlipresyna do leczenia zespołu wątrobowo-nerkowego typu 1
US9925233B2 (en) 2015-01-30 2018-03-27 Par Pharmaceutical, Inc. Vasopressin formulations for use in treatment of hypotension
JP2017014206A (ja) * 2015-06-30 2017-01-19 ナノアンティバイオティクス，インコーポレイテッド 腹水の治療
JP7579811B2 (ja) 2019-05-22 2024-11-08 バイオヴァイ インコーポレイテッド テルリプレシンの製剤

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WO2007144768A2 (fr) 2006-02-13 2007-12-21 Ferring B.V. Utilisation d'agonistes du récepteur de la vasopressine peptidiques
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GB1076984A (en) 1963-04-05 1967-07-26 Sandoz Ltd Improvements in or relating to local anaesthetics containing orn-vasopressin
US3352843A (en) 1963-08-30 1967-11-14 Sandoz Ltd Phe2-orn8-oxytocin
CS235151B1 (cs) 1982-08-26 1985-05-15 Michal Lebl Způsob dělení Dal isomerů analogů oxytocinu
US4829051A (en) 1983-04-05 1989-05-09 Vega Laboratories, Inc. N-substituted derivatives of 1-desaminovasopressin
US4483794A (en) 1983-05-10 1984-11-20 Ceskoslovenska Akademie Ved Analogs of neurohypophysial hormones
CS242062B1 (cs) 1984-08-23 1986-04-17 Milan Zaoral Vasopresinová a vasotocinová analoga a způsob jejich přípravy
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